Treatment of Tic Disorders in Children
Behavioral therapy, specifically Comprehensive Behavioral Intervention for Tics (CBIT) including habit reversal training and exposure with response prevention, should be the first-line treatment for children with functionally impairing tic disorders before considering any pharmacological options. 1, 2, 3
Initial Assessment and Diagnosis
Before initiating treatment, confirm the diagnosis by identifying core clinical features that distinguish tics from other conditions:
- Suppressibility - the child can temporarily hold back the tic 4, 1
- Distractibility - tics diminish when attention is diverted 4, 1
- Suggestibility - tics can be influenced by discussion or observation 4, 1
- Variability and waxing-waning pattern - tics change in frequency and severity over time 4, 1
- Premonitory sensations - uncomfortable urges preceding the tic (typically in children >8 years) 4, 1, 5
Critical pitfall to avoid: Do not misdiagnose tics as "habit behaviors" or "psychogenic symptoms"—these outdated terms lead to inappropriate interventions and treatment delays. 1, 3
Mandatory Comorbidity Screening
Screen every child with tic disorder for the following highly prevalent comorbidities, as they significantly impact treatment selection and outcomes:
- ADHD - present in 50-75% of children with tic disorders 1, 2, 3
- OCD or obsessive-compulsive behaviors - present in 30-60% of cases 1, 2, 3
- Anxiety and depressive disorders 6, 7
- Learning disabilities 4, 5
These comorbidities often cause more functional impairment than the tics themselves and must be addressed concurrently. 8
Treatment Algorithm
Step 1: Behavioral Interventions (First-Line)
CBIT should be offered as the initial treatment for all children with functionally impairing tics, particularly those with mild to moderate severity. 1, 3, 9
CBIT includes two core components:
- Habit reversal training (HRT) - teaching the child to perform a competing response when the premonitory urge occurs 1, 3, 6
- Exposure and response prevention (ERP) - deliberately experiencing premonitory sensations without performing the tic 1, 2, 6
Step 2: Pharmacological Treatment
Initiate medications when:
- Tics cause significant functional impairment, social problems, or pain 9, 7
- Behavioral therapy has failed or is not accessible 3, 9
- Tics are severe enough to interfere with daily activities 9, 7
First-Line Pharmacotherapy: Alpha-2 Adrenergic Agonists
Start with clonidine or guanfacine as the first medication, especially when ADHD or sleep disorders are comorbid, as these agents provide "around-the-clock" effects and may improve both tics and attention symptoms simultaneously. 1, 2, 3
Key prescribing details:
- Expect 2-4 weeks until therapeutic effects are observed 1
- Monitor pulse and blood pressure regularly 1
- Common adverse effects include somnolence, fatigue, and hypotension; administer in the evening to minimize daytime sedation 1
- These are uncontrolled substances, which is advantageous for long-term management 1
Second-Line Pharmacotherapy: Anti-Dopaminergic Medications
If alpha-2 agonists prove insufficient, use anti-dopaminergic medications including haloperidol, pimozide, risperidone, or aripiprazole. 1, 2, 3
Risperidone dosing specifics:
- Initial dose: 0.25 mg daily at bedtime 1
- Maximum dose: 2-3 mg daily in divided doses 1
- Monitor for extrapyramidal symptoms, which may occur at doses ≥2 mg daily 1
- Avoid coadministration with other QT-prolonging medications 1
Aripiprazole evidence:
- Demonstrated 56% positive response at 5 mg versus 35% on placebo in pediatric RCTs 1
- Effective dose range: 5-15 mg/day in children ages 6-17 1
- Showed significant improvements in irritability, hyperactivity, and stereotypy subscales 1
Critical safety warnings:
- Pimozide requires cardiac monitoring due to significant QT prolongation risk 1
- Typical antipsychotics should not be used as first-line due to higher risk of irreversible tardive dyskinesia 1
- Avoid benztropine or trihexyphenidyl for managing extrapyramidal symptoms in this population 1
Step 3: Managing Comorbid ADHD
When ADHD coexists with tics, use atomoxetine or guanfacine as preferred agents, as they may improve both conditions. 1
Stimulants can be used safely with proper informed consent:
- Multiple double-blind placebo-controlled studies demonstrate stimulants are highly effective for ADHD in children with tic disorders 1, 2
- Stimulants do not worsen tics in most cases 1, 2
- Methylphenidate is preferred over amphetamine-based medications, as amphetamines may worsen tic severity 1
Critical pitfall to avoid: Do not withhold stimulants in children with ADHD and tics based on outdated concerns about tic exacerbation. 1
Step 4: Treatment-Refractory Cases
A patient is considered treatment-refractory only after failing:
- Behavioral techniques (HRT and ERP) AND
- Therapeutic doses of at least three proven medications, including anti-dopaminergic drugs and alpha-2 adrenergic agonists 1, 3
Deep Brain Stimulation (DBS) criteria:
- Reserved exclusively for severe, treatment-refractory cases with significant functional impairment 1, 2, 3
- Requires stable, optimized treatment of comorbid conditions for at least 6 months 1, 3
- Recommended only for patients above 20 years of age due to uncertainty about spontaneous remission 1, 3
- Requires comprehensive assessment by a multidisciplinary team including neurologist, psychiatrist, and psychologist 1, 3
- Targets include centromedian-parafascicular thalamus and globus pallidus interna 1, 3
- Approximately 97% of published cases show substantial improvements 3
Prognostic Considerations
Nearly half of patients experience spontaneous remission by age 18, making watchful waiting reasonable in milder cases without functional impairment. 1, 9
- Less than 25% of individuals still have moderate or severe tics in adulthood 6
- Tic severity generally improves in late adolescence 4
Monitoring and Follow-Up
- Assess health-related quality of life using disease-specific instruments (e.g., GTS-QOL), as successful tic reduction does not always correlate with improved quality of life 1, 3
- Monitor for treatment adherence and psychosocial factors that could compromise outcomes 1
- Document impact on function and quality of life at each visit, as this is crucial for assessing treatment response 1
- Avoid excessive medical testing, as diagnosis is primarily clinical and unnecessary investigations cause iatrogenic harm 1, 3